Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease
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Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease. / Müller, Kathrin; Andersen, Peter M; Hübers, Annemarie; Marroquin, Nicolai; Volk, Alexander E; Danzer, Karin M; Meitinger, Thomas; Ludolph, Albert C; Strom, Tim M; Weishaupt, Jochen H.
In: BRAIN, Vol. 137, No. Pt 12, 01.12.2014, p. e309.Research output: SCORING: Contribution to journal › Other (editorial matter etc.) › Research
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TY - JOUR
T1 - Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease
AU - Müller, Kathrin
AU - Andersen, Peter M
AU - Hübers, Annemarie
AU - Marroquin, Nicolai
AU - Volk, Alexander E
AU - Danzer, Karin M
AU - Meitinger, Thomas
AU - Ludolph, Albert C
AU - Strom, Tim M
AU - Weishaupt, Jochen H
N1 - Document Type: Letter
PY - 2014/12/1
Y1 - 2014/12/1
KW - Amyotrophic Lateral Sclerosis
KW - DNA, Mitochondrial
KW - Female
KW - Frontotemporal Dementia
KW - Humans
KW - Male
KW - Mitochondria
KW - Mitochondrial Diseases
KW - Mitochondrial Proteins
U2 - 10.1093/brain/awu227
DO - 10.1093/brain/awu227
M3 - Other (editorial matter etc.)
C2 - 25113787
VL - 137
SP - e309
JO - BRAIN
JF - BRAIN
SN - 0006-8950
IS - Pt 12
ER -